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The Nephrotic Syndrome Foundation is a non-profit organization supporting those diagnosed with Nephrotic Syndrome, their families and the ongoing search for a cure.

Background: Nephrotic Syndrome is a serious and rare auto-immune disease that attacks the kidneys causing them to shut down. There is no known cause or cure. Treatments are extremely limited and consist primarily of steroids, cancer, and transplant medications. Many patients are children who spend a major part of their life in and out of the hospital, trying to find a treatment that keeps them in remission while managing the side effects. Receiving this diagnosis is life-changing. It can take the breath out of any parent or child who finds themselves in this situation. Our goal at NSF is to meet each family and child in these tough times and lift each one up as best we can by providing financial and emotional support to help them weather the times to better health, acceptance, and adjustment.

President and Founders:

Andi and Tucker Callaway

NSF Advisory Board:

Laura Markstein

Tita Forrest

Annabel Chynces

Dr. Paul Brakeman

Contact Us - we want to hear from you!

Donations via check should be made out to 'Social Good Fund / NSF' and sent to:


The Nephrotic Syndrome Foundation

c/o Andrea Callaway

325 Marks Road

Alamo, CA 94507

The Nephrotic Syndrome Foundation is a fiscally sponsored project by Social Good Fund, a California non-profit corporation and registered 501(c)(3) organization, Tax ID (EIN) 46-1323531.


Donations are tax-deductible to the fullest extent of the law.  

For questions or to get involved, contact us at

Thank you for your support!

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